TY - JOUR
T1 - Engineering patient-specific bioprinted constructs for treatment of degenerated intervertebral disc
AU - Costa, João Bebiano
AU - Silva-Correia, Joana
AU - Ribeiro, Viviana Pinto
AU - da Silva Morais, Alain
AU - Oliveira, Joaquim Miguel
AU - Reis, Rui Luís
N1 - Funding Information:
The authors would like to acknowledge the financial support provided by the Portuguese Foundation for Science and Technology (FCT) through the project EPIDisc (UTAP-EXPL/BBBECT/0050/2014), funded in the Framework of the “International Collaboratory for Emerging Technologies, CoLab”, UT Austin|Portugal Program. FCT is also greatly acknowledged for the distinctions attributed to J. Silva-Correia (IF/00115/2015) and J. M. Oliveira (IF/00423/2012 and IF/01285/2015) under the Investigator FCT program. V.P. Ribeiro was awarded a PhD scholarship (PD/BD/113806/2015) under the financial support from FCT/MCTES and FSE/POCH , PD/59/2013. FCT/MCTES is also acknowledged for the PhD scholarship attributed to J. B. Costa (PD/BD/113803/2015).
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2019/6
Y1 - 2019/6
N2 - Lower back pain (LBP), which is strongly associated with intervertebral disc (IVD)degeneration, is one of the most frequently reported age- and work-related disorder in actual society, leading to a huge socio-economic impact worldwide. The current treatments have poor clinical outcomes and do not consider each patient needs. Thus, there is a growing interest in the potential of personalized cell-based tissue engineering (TE)approaches aimed to regenerate the damaged IVD and efficiently restore full disc function. In this work, a bioink composed by silk fibroin (SF)hydrogel combined with elastin was used to bioprint patient-specific substitutes mimicking IVD ultrastructure, in particular the outer region of the IVD (i.e. annulus fibrosus, AF). Following a reverse engineering approach, the proposed strategy makes use of a 3D model of AF obtained by semi-automatic morphological segmentation from magnetic resonance imaging dataset of human IVD. SF/elastin bioprinted scaffolds were characterized thoroughly in vitro, in terms of physico-chemical and biological performance. The bioprinted SF/elastin scaffolds were shown to possess structural and mechanical properties similar to the native AF and to support cell attachment and growth. Human adipose-derived stem cell cultured onto the SF/elastin bioprinted scaffolds were shown to adhere, proliferate and maintain metabolic activity and viability up to 21 days of culturing. The implantation of custom-made SF/elastin implants that best emulate a patient AF anatomy can potentially open up new personalized treatments for tackling IVD disorders by means of improving recovery time after surgery and helping to restore spine biofunctionality.
AB - Lower back pain (LBP), which is strongly associated with intervertebral disc (IVD)degeneration, is one of the most frequently reported age- and work-related disorder in actual society, leading to a huge socio-economic impact worldwide. The current treatments have poor clinical outcomes and do not consider each patient needs. Thus, there is a growing interest in the potential of personalized cell-based tissue engineering (TE)approaches aimed to regenerate the damaged IVD and efficiently restore full disc function. In this work, a bioink composed by silk fibroin (SF)hydrogel combined with elastin was used to bioprint patient-specific substitutes mimicking IVD ultrastructure, in particular the outer region of the IVD (i.e. annulus fibrosus, AF). Following a reverse engineering approach, the proposed strategy makes use of a 3D model of AF obtained by semi-automatic morphological segmentation from magnetic resonance imaging dataset of human IVD. SF/elastin bioprinted scaffolds were characterized thoroughly in vitro, in terms of physico-chemical and biological performance. The bioprinted SF/elastin scaffolds were shown to possess structural and mechanical properties similar to the native AF and to support cell attachment and growth. Human adipose-derived stem cell cultured onto the SF/elastin bioprinted scaffolds were shown to adhere, proliferate and maintain metabolic activity and viability up to 21 days of culturing. The implantation of custom-made SF/elastin implants that best emulate a patient AF anatomy can potentially open up new personalized treatments for tackling IVD disorders by means of improving recovery time after surgery and helping to restore spine biofunctionality.
KW - 3D printing
KW - Intervertebral disc
KW - Patient-specific
KW - Reverse engineering
KW - Silk fibroin/elastin bioink
KW - Tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=85059048029&partnerID=8YFLogxK
U2 - 10.1016/j.mtcomm.2018.01.011
DO - 10.1016/j.mtcomm.2018.01.011
M3 - Article
SN - 2352-4928
VL - 19
SP - 506
EP - 512
JO - Materials Today Communications
JF - Materials Today Communications
ER -